Treating hematological malignancies with cell therapy: where are we now?

被引:20
|
作者
Landoni, Elisa [1 ]
Savoldo, Barbara [1 ,2 ]
机构
[1] Univ N Carolina, Lineberger Comprehens Canc Ctr, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Dept Pediat, Chapel Hill, NC 27599 USA
关键词
Adoptive cell therapy; hematologic malignancies; T cell receptor; chimeric antigen receptor; transgenic TCR; CAR T cells; CHIMERIC ANTIGEN RECEPTOR; CAR-T-CELLS; ENHANCED ANTITUMOR-ACTIVITY; B-CELL; ADOPTIVE IMMUNOTHERAPY; CD19; CAR; CHECKPOINT BLOCKADE; MATURATION ANTIGEN; HUMAN-LYMPHOCYTES; MYELOID-LEUKEMIA;
D O I
10.1080/14712598.2018.1384810
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Introduction: Adoptive cell therapy (ACT) is becoming an increasingly successful and widespread form of treatment for different types of cancer. Compared to chemotherapy or monoclonal antibodies, ACT is an active biological strategy, with infused immune cells featuring dynamic migration, expansion and long-term persistence properties. ACT in hematological malignancies offered the initial proof of principle of the feasibility for this innovative 'live-drug'. Areas covered: In this review, the authors summarize the clinical results achieved with two specific strategies in hematological malignancies: chimeric antigen receptor (CAR) and T cell receptor (transgenic TCR) redirected T cells. Moreover, they discuss the recent pre-clinical studies aimed at increasing the feasibility, safety and efficacy of ACT. Expert opinion: ACT can promote cancer regression in patients with leukemia, lymphoma and multiple myeloma. Nevertheless, more precise targeting of tumor cells and containment of side effects are needed. Overcoming tumor-associated immunosuppressive mechanisms and preventing tumor escape are also emerging as critical barriers. Finally, simplification in the manufacturing procedures should promote wider application of these technologies outside academic centers. Although the enthusiasm for ACT-based therapies is high, comprehensive and systematic clinical studies are required to advance the field.
引用
收藏
页码:65 / 75
页数:11
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